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[波兰家族性结节病中由DRB基因编码的人类白细胞抗原II类抗原的多态性]

[Polymorphism of histocompatibility class II antigens coded with the DRB gene in in familial sarcoidosis in Poland].

作者信息

Goljan A, Puścińska E, Sankowska M, Zieliński J

机构信息

Kliniki Chorób Płuc Instytutu Gruźlicy i Chorób Płuc, Warszawie.

出版信息

Pneumonol Alergol Pol. 2000;68(11-12):533-44.

Abstract

Several studies suggested association between some human leukocyte antigen (HLA) alleles and sarcoidosis, but none has been conclusive. To confirm possible association of sarcoidosis with HLA-DRB1, -DRB3,- DRB4, -DRB5 associated alleles HLA-DR genotyping was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method in 17 polish families with familial sarcoidosis and in 101 healthy controls. The families with sarcoidosis consisted of 31 affected first-degree relatives from 16 families, 2 affected cousins from 1 family and 78 healthy relatives of those patients. We found 3 varieties of familial sarcoidosis: a) in parent and offspring (5 pairs), b) in siblings (10 sib pairs and 1 sib triplet) and in cousins (1 family). Genotyping for HLA-DRB1,-DRB3,-DRB4,-DRB5 revealed an over-representation of HLA-DR5(12) and DRw52 among antigens shared by affected relatives comparing to the control group. A significant increase in the frequency of HLA-DR7 and HLA-DRw53 antigens (p < 0.05) was found in subjects from the control group. Comparing the group of family members (affected and healthy relatives taken together, n = 111) with the control group (n = 101) we found a significant differences in the distribution of HLA-DR2(15), HLA-DR5(12), HLA-DR6, HLA-DR9 and HLA-DRw52. Those antigens were more frequent (p < 0.05) in members from families with sarcoidosis. The frequencies of HLA-DR1, HLA-DR2(16), HLA-DR7 and HLA-DRw53 were significantly higher (p < 0.05) in the control group. Presented results suggest that HLA-DRB alleles contribute to the susceptibility to sarcoidosis in the Polish population.

摘要

多项研究表明某些人类白细胞抗原(HLA)等位基因与结节病之间存在关联,但尚无定论。为了证实结节病与HLA-DRB1、-DRB3、-DRB4、-DRB5相关等位基因的可能关联,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,对17个患有家族性结节病的波兰家庭和101名健康对照者进行了HLA-DR基因分型。患有结节病的家庭包括来自16个家庭的31名受影响的一级亲属、来自1个家庭的2名受影响的表亲以及这些患者的78名健康亲属。我们发现了3种家族性结节病类型:a)父母与子女(5对),b)兄弟姐妹(10对同胞和1个同胞三联体)以及表亲(1个家庭)。对HLA-DRB1、-DRB3、-DRB4、-DRB5进行基因分型显示,与对照组相比,受影响亲属共有的抗原中HLA-DR5(12)和DRw52的比例过高。在对照组受试者中发现HLA-DR7和HLA-DRw53抗原的频率显著增加(p < 0.05)。将家庭成员组(受影响和健康亲属合计,n = 111)与对照组(n = 101)进行比较,我们发现HLA-DR2(15)、HLA-DR5(12)、HLA-DR6、HLA-DR9和HLA-DRw52的分布存在显著差异。这些抗原在患有结节病的家庭成员中更为常见(p < 0.05)。HLA-DR1、HLA-DR2(16)、HLA-DR7和HLA-DRw53在对照组中的频率显著更高(p < 0.05)。呈现的结果表明,HLA-DRB等位基因有助于波兰人群对结节病的易感性。

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